Back to Search Start Over

A Novel Circulating Noncoding Small RNA for the Detection of Acute Myocarditis

Authors :
Mario Plebani
Raquel Sánchez-Díaz
Roberto Martín-Asenjo
Rafael Blanco-Domínguez
Isidoro González-Álvaro
Adela Matesanz-Marín
Hortensia de la Fuente
María L. Martín-Mariscal
Ane M. Salvador-Garicano
Leticia Fernández-Friera
Bettina Heidecker
Mercedes Ricote
Katelyn A. Bruno
Sam A. Michelhaugh
Borja Ibanez
Domingo A. Pascual-Figal
Thomas F. Lüscher
Mara Seguso
Marcos M. García-Guimaraes
Pilar Martín
Luisa M. Villar-Guimerans
Nasrien E. Ibrahim
Guillermo Moreno
Alida L.P. Caforio
Valentin Fuster
Anna Baritussio
Laura Alonso-Herranz
Jan Kottwitz
Marta Relaño
Katerina Tsilingiri
E. Daudén
Héctor Bueno
Rosa Jiménez-Alejandre
Beatriz Linillos-Pradillo
James L. Januzzi
Cristina Basso
Amaia Martínez-León
Renzo Marcolongo
Francisco Sánchez-Madrid
Sabino Iliceto
F. Alfonso
Luis Jesús Jiménez-Borreguero
Saumya Das
De Lisa Fairweather
Source :
New England Journal of Medicine. 384:2014-2027
Publication Year :
2021
Publisher :
Massachusetts Medical Society, 2021.

Abstract

Background The diagnosis of acute myocarditis typically requires either endomyocardial biopsy (which is invasive) or cardiovascular magnetic resonance imaging (which is not universally available). Additional approaches to diagnosis are desirable. We sought to identify a novel microRNA for the diagnosis of acute myocarditis. Methods To identify a microRNA specific for myocarditis, we performed microRNA microarray analyses and quantitative polymerase-chain-reaction (qPCR) assays in sorted CD4+ T cells and type 17 helper T (Th17) cells after inducing experimental autoimmune myocarditis or myocardial infarction in mice. We also performed qPCR in samples from coxsackievirus-induced myocarditis in mice. We then identified the human homologue for this microRNA and compared its expression in plasma obtained from patients with acute myocarditis with the expression in various controls. Results We confirmed that Th17 cells, which are characterized by the production of interleukin-17, are a characteristic feature of myocardial injury in the acute phase of myocarditis. The microRNA mmu-miR-721 was synthesized by Th17 cells and was present in the plasma of mice with acute autoimmune or viral myocarditis but not in those with acute myocardial infarction. The human homologue, designated hsa-miR-Chr8:96, was identified in four independent cohorts of patients with myocarditis. The area under the receiver-operating-characteristic curve for this novel microRNA for distinguishing patients with acute myocarditis from those with myocardial infarction was 0.927 (95% confidence interval, 0.879 to 0.975). The microRNA retained its diagnostic value in models after adjustment for age, sex, ejection fraction, and serum troponin level. Conclusions After identifying a novel microRNA in mice and humans with myocarditis, we found that the human homologue (hsa-miR-Chr8:96) could be used to distinguish patients with myocarditis from those with myocardial infarction. (Funded by the Spanish Ministry of Science and Innovation and others.).

Details

ISSN :
15334406 and 00284793
Volume :
384
Database :
OpenAIRE
Journal :
New England Journal of Medicine
Accession number :
edsair.doi...........d03b9480e394b86e66f8a6b6a488ae3f